Total Synthesis of Kopsinitarine E

被引:21
|
作者
Nagaraju, Karre [1 ]
Ni, Dongshun [1 ]
Ma, Dawei [1 ]
机构
[1] Univ Chinese Acad Sci, Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Bioorgan & Nat Prod Chem,Ctr Excell, 345 Lingling Lu, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
cyclization; indole alkaloids; Mannich reaction; semi-pinacol rearrangement; total synthesis; CATALYZED DECARBOXYLATIVE ALLYLATION; CARBOXYLIC-ACID DERIVATIVES; CONCISE TOTAL-SYNTHESIS; INDOLE ALKALOIDS; SEMIPINACOL REARRANGEMENT; CHEMOSELECTIVE REDUCTION; NATURAL-PRODUCTS; MANNICH REACTION; TERTIARY AMIDES; KOPSIA-TENUIS;
D O I
10.1002/anie.202011093
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Kopsinitarines A-E are complex octacyclic cagedKopsiaalkaloids with strained cage skeletons and a unique cyclic hemiaminal bridge that makes total synthesis challenging. Herein, we disclose the first total synthesis of kopsinitarine E. The key synthetic features include a SmI2-mediated radical cascade cyclization and a subsequent semi-pinacol rearrangement to install the key carbocyclic skeleton, a chemoselective hydrosilyl amide reduction to construct the hemiaminal ether bridge, and an intramolecular Mannich reaction to establish the highly strained cage system.
引用
收藏
页码:22039 / 22042
页数:4
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